|
NM_145064.3:c.432+4A>T
MANE Select
|
NP_659501.1:n.432+4A>T
|
|
ENST00000332782.7:c.432+4A>T
MANE Select
|
ENSP00000329200.2:n.432+4A>T
|
|
NM_001286256.1:c.315+4A>T
|
NP_001273185.1:n.315+4A>T
|
|
NM_001286256.2:c.315+4A>T
|
NP_001273185.1:n.315+4A>T
|
|
NM_001286257.1:c.-126-504A>T
|
NP_001273186.1:n.-126-504A>T
|
|
NM_001286257.2:c.-126-504A>T
|
NP_001273186.1:n.-126-504A>T
|
|
NM_145064.2:c.432+4A>T
|
NP_659501.1:n.432+4A>T
|
|
NR_104422.1:n.202-504A>T
|
|
|
NR_104422.2:n.196-504A>T
|
|
|
ENST00000332782.6:c.432+4A>T
|
ENSP00000329200.2:n.432+4A>T
|
|
ENST00000546246.2:c.-126-504A>T
|
ENSP00000441515.2:n.-126-504A>T
|
|
ENST00000553489.1:c.432+4A>T
|
ENSP00000452299.1:n.432+4A>T
|
|
ENST00000554578.5:c.315+4A>T
|
ENSP00000452068.1:n.315+4A>T
|
|
ENST00000557176.5:c.-126-504A>T
|
ENSP00000450740.1:n.-126-504A>T
|
|
XM_011538126.1:c.432+4A>T
|
XP_011536428.1:n.432+4A>T
|
|
XM_011538126.2:c.432+4A>T
|
XP_011536428.1:n.432+4A>T
|
|
XR_002957305.1:n.628+4A>T
|
|
|
XR_944515.1:n.628+4A>T
|
|
|
XR_944515.2:n.628+4A>T
|
|